Biological Functions of the Low and High Molecular Weight Protein Isoforms of Fibroblast Growth Factor-2 in Cardiovascular Development and Disease

被引：72
作者：
Liao, Siyun
Bodmer, Janet
Pietras, Daniel
Azhar, Mohamad [2 ,3 ]
Doetschman, Tom [2 ,3 ]
Schultz, Jo El J. [1 ]
机构：
[1] Univ Cincinnati, Coll Med, Dept Pharmacol & Cell Biophys, Cincinnati, OH 45267 USA
[2] Univ Arizona, Inst BIO5, Tucson, AZ USA
[3] Univ Arizona, Dept Cell Biol & Anat, Tucson, AZ USA
来源：
DEVELOPMENTAL DYNAMICS | 2009年 / 238卷 / 02期
关键词：
fibroblast growth factor; low and high molecular weight isoforms; ischemia-reperfusion injury; cardiac hypertrophy; vascular biology; cardiovascular development; myocardial development; epicardium; epicardium-derived cells; heart valves; coronary vessels; smooth muscle cells; aortic arch; cardiac fibroblasts; transgenic and knockout mouse models; CARDIAC-SPECIFIC OVEREXPRESSION; THERAPEUTIC ANGIOGENESIS; NUCLEAR-LOCALIZATION; ISCHEMIC-HEART; FACTOR BFGF; CELL-DEATH; HYPERTROPHIC RESPONSE; MYOCARDIAL-INFARCTION; CHROMATIN COMPACTION; NUCLEOTIDE-SEQUENCE;
D O I：
10.1002/dvdy.21677
中图分类号：
R602 [外科病理学、解剖学]; R32 [人体形态学];
学科分类号：
100101 ;
摘要：
Fibroblast growth factor 2 (FGF2) consists of multiple protein isoforms (low molecular weight, LAM, and high molecular weight, HAW) produced by alternative translation from the Fgt2 gene. These protein isoforms are localized to different cellular compartments, indicating unique biological activity. FGF2 isoforms in the heart have distinct roles in many pathological circumstances in the heart including cardiac hypertrophy, ischemia-reperfusion injury, and atherosclerosis. These studies suggest distinct biological activities of FGF2 LAM and HMW isoforms both in vitro and in vivo. Yet, due to the limitations that only the recombinant FGF2 LMW isoform is readily available and that the FGF2 antibody is nonspecific with regards to its isoforms, much remains to be determined regarding the role(s) of the FGF2 LMW and HMW isoforms in cellular behavior and in cardiovascular development and pathophysiology. This review summarizes the activities of LMW and HMW isoforms of FGF2 in cardiovascular development and disease. Developmental Dynamics 238:249-264, 2009. (c) 2008 Wiley-Liss, Inc.
引用
收藏
页码：249 / 264
页数：16
相关论文
共 167 条
[1]   HUMAN BASIC FIBROBLAST GROWTH-FACTOR - NUCLEOTIDE-SEQUENCE, GENOMIC ORGANIZATION, AND EXPRESSION IN MAMMALIAN-CELLS [J].
ABRAHAM, JA ;
WHANG, JL ;
TUMOLO, A ;
MERGIA, A ;
FIDDES, JC .
COLD SPRING HARBOR SYMPOSIA ON QUANTITATIVE BIOLOGY, 1986, 51 :657-668
[2]  
[Anonymous], 2007, Heart and Stroke Statistical Update
[3]   Augmented expression of cardiotrophin-1 and its receptor component, gp130, in both left and right ventricles after myocardial infarction in the rat [J].
Aoyama, T ;
Takimoto, Y ;
Pennica, D ;
Inoue, R ;
Shinoda, E ;
Hattori, R ;
Yui, Y ;
Sasayama, S .
JOURNAL OF MOLECULAR AND CELLULAR CARDIOLOGY, 2000, 32 (10) :1821-1830
[4]   Nuclear activities of basic fibroblast growth factor: Potentiation of low-serum growth mediated by natural or chimeric nuclear localization signals [J].
Arese, M ;
Chen, Y ;
Florkiewicz, RZ ;
Gualandris, A ;
Shen, B ;
Rifkin, DB .
MOLECULAR BIOLOGY OF THE CELL, 1999, 10 (05) :1429-1444
[5]  
Arnaud E, 1999, MOL CELL BIOL, V19, P505
[6]  
ASKEW DS, 1993, HEMATOL PATHOL, V7, P1
[7]   Transforming growth factor beta in cardiovascular development and function [J].
Azhar, M ;
Schultz, JEJ ;
Grupp, I ;
Dorn, GW ;
Meneton, P ;
Molin, DGM ;
Gittenberger-de Groot, AC ;
Doetschman, T .
CYTOKINE & GROWTH FACTOR REVIEWS, 2003, 14 (05) :391-407
[8]   ENHANCED ANGIOGENESIS AND GROWTH OF COLLATERALS BY INVIVO ADMINISTRATION OF RECOMBINANT BASIC FIBROBLAST GROWTH-FACTOR IN A RABBIT MODEL OF ACUTE LOWER-LIMB ISCHEMIA - DOSE-RESPONSE EFFECT OF BASIC FIBROBLAST GROWTH-FACTOR [J].
BAFFOUR, R ;
BERMAN, J ;
GARB, JL ;
RHEE, SW ;
KAUFMAN, J ;
FRIEDMANN, P .
JOURNAL OF VASCULAR SURGERY, 1992, 16 (02) :181-191
[9]   Biological roles of fibroblast growth factor-2 [J].
Bikfalvi, A ;
Klein, S ;
Pintucci, G ;
Rifkin, DB .
ENDOCRINE REVIEWS, 1997, 18 (01) :26-45
[10]  
BOUCHE G, 1994, CELL MOL BIOL RES, V40, P547
12345678910